Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
  • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
  • A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
  • A61L15/22—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
  • A61L15/28—Polysaccharides or their derivatives
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
  • A61L2400/00—Materials characterised by their function or physical properties
  • A61L2400/04—Materials for stopping bleeding
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
  • Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
  • Y10T442/2525—Coating or impregnation functions biologically [e.g., insect repellent, antiseptic, insecticide, bactericide, etc.]

Definitions

• the present invention relates to wound dressings, e.g. hemostatic wound dressings, containing or fabricated in part from an aldehyde-modified, polysaccharide, e.g. a biodegradable aldehyde-modified regenerated cellulose, and to methods of using such wound dressings.
• wound dressings e.g. hemostatic wound dressings
• polysaccharide e.g. a biodegradable aldehyde-modified regenerated cellulose
• ORC Oxidized regenerated cellulose, as described herein below and commonly referred to as ORC, due to its biodegradability, bactericidal, and hemostatic properties, has long been used as a hemostatic wound dressing in a variety of surgical procedures, including neurosurgery, abdominal surgery, cardiovascular surgery, thoracic surgery, head and neck surgery, pelvic surgery, and skin and subcutaneous tissue procedures.
• ORC as recognized heretofore by those skilled in the art of wound dressings, is carboxylic-oxidized, regenerated cellulose comprising reactive carboxylic acid groups.
• the oxidized cellulose is carboxyl-modified to contain a certain amount of carboxylic acid moieties.
• hemostatic ORC absorbable hemostats commercially available include Surgicel® absorbable hemostat, a knitted fabric of ORC; Surgicel Nu-Knit® absorbable hemostat, a dense ORC fabric; and Surgicel® Fibrillar absorbable hemostat; all available from Johnson & Johnson Wound Management Worldwide, a division of Ethicon, Inc., Somerville, N.J., a Johnson & Johnson Company.
• Other examples of commercial absorbable hemostats containing carboxyl-oxidized cellulose include Oxycel® absorbable cellulose surgical wound dressing, available from Becton Dickinson, Morris Plains, N.J.
• oxidized cellulose (OC) and oxidized regenerated cellulose (ORC) hemostats noted above are knitted or non-woven fabrics comprising carboxylic acid groups, as noted above, in amounts effective to provide them with anti-microbial properties.
• the acid-based ORC and OC due to their acidic pH, also rapidly denatures acid-sensitive, hemostatic proteins, including thrombin or fibrinogen, on contact.
• the OC or ORC as a carrier for acid-sensitive species, such as thrombin and fibrinogen, as well as other acid-sensitive biologics and pharmaceutical agents.
• oxidized cellulose generally referred to as oxycellulose
• Oxidation of the secondary alcohol groups of cellulose with periodic acid or its salts to form a aldehyde-modified cellulose has been disclosed in the prior art as a means of characterizing the chemical structure of mono-, oligo- and polysaccharide-based materials.
• aldehyde-modified cellulose has not been utilized in wound dressings to provide hemostasis.
• Methods of producing highly oxidized tri-carboxylic acid derivatives of cellulose as hemostic materials involving two-stage oxidation by successive processing with an iodine-containing compound and nitrogen oxides, has been disclosed in RU2146264 and IN159322.
• oxidized cellulosic materials were prepared by preliminary oxidation with metaperiodate or periodic acid to yield periodate-oxidized, dialdehyde cellulose to form the intermediate for forming OC.
• dialdehyde cellulose intermediate then is further oxidized by NO 2 to yield the OC with a higher carboxylic acid content, which is suitable for use as a hemostatic, anti-microbial and wound healing agent.
• the disclosures do not, however, suggest or disclose that the periodate-oxidized, dialdehyde cellulose intermediate formed in the first stage oxidation may or should be used in the preparation of wound dressings, e.g. hemostatic wound dressings.
• hemostatic wound dressing that not only provides hemostasis and anti-microbial properties similar to conventional OC-containing hemostatic wound dressings, but that also is compatible with acid-sensitive species, such as thrombin and fibrinogen. To date, no such wound dressing has been reported.
• the present invention provides such a wound dressing that not only provides hemostatic and anti-microbial properties equivalent to conventional ORC-based hemostatic wound dressings, but that also is compatible with “acid-sensitive” species.
• the present invention is directed to hemostatic wound dressings that include a substrate for contacting a wound, which substrate comprises a wound-contacting surface, and which substrate comprises and is fabricated at least in part from a biocompatible, aldehyde-modified polysaccharide.
• the aldehyde-modified polysaccharide preferably comprises an amount of aldehyde moieties effective to render the substrate biodegradable.
• the wound dressings provide and maintain effective hemostasis to a wound in need of hemostasis.
• the invention also is directed to methods of providing hemostasis to a wound, which method includes applying to a wound requiring hemostasis the wound dressing described herein.
• the present invention is directed to hemostatic wound dressings that provide and maintain effective hemostasis when applied to a wound requiring hemostasis.
• Effective hemostasis is the ability to control and/or abate capillary, venous, or arteriole bleeding within an effective time, as recognized by those skilled in the art of hemostasis.
• the wound dressings of the present invention provide hemostasis within about fifteen minutes, and more preferably twelve minutes, from the time the wound dressing is applied to the wound.
• the hemostatic dressings of the present invention are particularly useful when conventional procedures to control and/or abate bleeding, such as pressure or suturing, are either ineffective or impractical.
• the hemostats of the present invention also are useful where one desires to utilize in, or in conjunction with, the wound dressing hemostatic agents, or other biological or therapeutic compounds, moieties or species, particularly those “acid-sensitive” adjuncts that may be degraded or denatured by, or otherwise detrimentally affected by acidic pH provided by, e.g. carboxylic acid moieties, such as is provided by conventional hemostats.
• the wound dressings may take various physical forms and may include, without limitation, fibrous or non-fibrous, woven or non-woven dressings.
• the wound dressing may comprise a fiber, including microfibers, a film, a fabric, a foam, a bead, a gel, or combinations thereof. Regardless of the form of the wound dressing, it will comprise a substrate for contacting and/or covering the wound.
• substrates may be incorporated into slurries, pastes, dispersions or other mixtures and applied directly to a wound surface.
• additional wound dressings may be applied over such substrates, but are not necessarily required.
• the wound dressing could comprise the substrate in a carrier for delivery of the substrate to the wound.
• polymeric beads, microfibers, or ground foam substrates all comprising the aldehyde-modified polysaccharides of the present invention, may be dispersed in slurries or dispersions that may be applied directly to a wound or, in certain circumstances, injected subcutaneously or otherwise disposed internally into the body to provide hemostasis.
• Gels also may be formulated so as to be applied to a wound or otherwise disposed within the body in order to provide hemostasis.
• the dressing may consist essentially of the substrate, or may consist of the substrate. This is particularly true where the wound dressing is fabricated from a knitted, woven or non-woven hemostatic fabric that has been oxidized to provide aldehyde modification, as described herein, and which serves as the substrate for the wound dressing. In those cases, while the wound dressing may further include such components as backing layers, adhesive layers, or the like, the wound dressing can include only the hemostatic fabric.
• the wound dressing substrate will comprise a wound-contacting surface.
• Such substrates may take various physical forms, including, but not limited to, fibrous or non-fibrous, woven or non-woven substrates.
• the wound dressing substrates may comprise a fiber, including microfibers, a film, a fabric, a foam, a bead, a gel, or combinations thereof.
• the substrate comprises a knitted fabric. The fabric may be formed, cut or otherwise shaped to cover the wound surface, thereby providing protection of the wound from physical trauma and effective hemostasis of the wound.
• Wound dressings of the present invention and more particularly the wound-contacting substrates thereof, comprise a biocompatible, aldehyde-modified polysaccharide.
• the polysaccharide will contain an amount of aldehyde moieties effective to render the modified polysaccharide biodegradable, meaning that the polysaccharide is degradable by the body into components that either are resorbable by the body, or that can be passed readily by the body. More particularly, the biodegraded components do not elicit permanent chronic foreign body reaction because they are absorbed by the body, such that no permanent trace or residual of the component is retained at the implantation site.
• Aldehyde-modified polysaccharides used in the present invention may be prepared from biocompatible polysaccharides that are useful in medical devices.
• Such polysaccharides include, without limitation, cellulose, alkyl cellulose, e.g.
• the polysaccharide is oxidized as described herein to assure that the aldehyde-modified polysaccharide is biodegradable.
• biodegradable, aldehyde-modified polysaccharides may be represented by Structure I below.
• x and y represent mole percent, x plus y equals 100 percent, x is from about 95 to about 5, y is from about 5 to about 95; and R may be CH 2 OR 3 , COOR 4 , sulphonic acid, or phosphonic acid; R 3 and R 4 may be H, alkyl, aryl, alkoxy or aryloxy, and R 1 and R 2 may be H, alkyl, aryl, alkoxy, aryloxy, sulphonyl or phosphoryl.
• the biocompatible, biodegradable hemostatic wound dressing comprises a wound contacting/covering substrate prepared from a biocompatible, biodegradable, aldehyde-modified regenerated cellulose.
• Regenerated cellulose is preferred due to its higher degree of uniformity versus cellulose that has not been regenerated. Regenerated cellulose is described in, for instance, U.S. Pat. No. 3,364,200, the contents of which is hereby incorporated by reference as if set forth in its entirety.
• preferred aldehyde-modified regenerated cellulose is one comprising repeating units of Structure II:
• x and y represent mole percent, x plus y equals 100 percent, x is from about 95 to about 5, y is from about 5 to about 95; and R is CH 2 OH, R 1 and R 2 are H.
• x is from about 90 to 10 and y is about 10 to about 90.
• x is from about 80 to 20 and y is from about 20 to about 80.
• x is from about 70 to about 30.
• x is about 70 and y is about 30.
• the hemostatic dressings of the present invention also provide anti-microbial activities due to the presence of effective amounts of the aldehyde moieties. It has been shown that in spite of being non-acidic, the aldehyde-modified regenerated cellulose is anti-microbial in nature.
• the hemostats of the present invention were found to be significantly effective against microorganisms, such as Methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa , etc.
• MRSA Methicillin-resistant Staphylococcus aureus
• Pseudomonas aeruginosa etc.
• the anti-microbial activities of the non-acidic aldehyde-modified regenerated cellulose are shown to be comparable to those of the acidic carboxylic oxidized regenerated cellulose conventionally used.
• the acidic carboxylic oxidized regenerated cellulose loses its anti-microbial activities upon neutralization reaction or over a period of time as the acid groups are neutralized in the body.
• the aldehyde-modified regenerated cellulose utilized in the present invention is expected to retain its anti-microbial activity over a longer period of time.
• the aldehyde-modified regenerated polysaccharide is essentially free of functional or reactive moieties other than aldehyde moieties.
• essentially free it is meant that the polysaccharide does not contain such functional or reactive moieties in amounts effective to alter the properties of the aldehyde-modified polysaccharide or to provide the substrate comprising the polysaccharide with a pH of less than about 4.5, more preferably less than about 5, or greater than about 9, preferably about 9.5.
• Such moieties include, without limitation, carboxylic acid moieties typically present on wound dressings made from OC.
• carboxylic acid moieties will lower the pH of the substrates and dressings so that they are not compatible for use with those species that may be degraded or denatured by such a low pH, e.g. thrombin.
• Other undesired moieties include, without limitation, sulfonyl or phosphonyl moieties.
• the hemostat of the present invention exhibits increased thermal stability compared to that of the carboxylic oxidized regenerated cellulose fabric (ORC).
• the increased thermal stability may be indicative of improved physical shelf-life, compared to ORC or neutralized ORC.
• the fabrics utilized in the present invention may be knitted, woven, or non-woven, provided that the fabric possesses the physical properties adequate for wound dressings, in general, and hemostasic wound dressings, specifically. Fabrics oxidized by periodic acid or its salts described in the present invention are expected to retain physical properties and mechanical integrity required for use in wound dressings. Hemostatic fabrics useful for use in hemostatic wound dressings according to the present invention include fabrics comprising the aldehyde-modified polysaccharides of the present invention. Structures that are useful in the present invention include those described in U.S. Pat. Nos.
• the hemostatic wound dressing of the present invention comprises as the wound contacting/covering hemostatic substrate a warp knitted tricot fabric constructed of bright rayon yarn that has been oxidized by periodic acid or its salts such that the substrate comprises aldehyde moieties.
• SEM Scanning Electron Microscopic
• the hemostat of the present invention remains very flexible, conforms to a bleeding site, and retains good tensile and compressive strength to withstand handling during application.
• the aldehyde-modified regenerated cellulose hemostat can be cut into different sizes and shapes to fit the surgical needs. It can be rolled up or packed into irregular anatomic areas.
• a biologics, a drug, or a combination of pharmaceutical agents may be incorporated into certain wound dressings of the present invention without having to adjust pH prior to incorporation into the dressing.
• a drug or agent first may be dissolved in an appropriate solvent. The fabric is then coated with the drug solution and the solvent is removed.
• Preferred biologics, drugs and agent include analgesics, anti-infective agents, antibiotics, adhesion preventive agents, pro-coagulants, and wound healing growth factors.
• the aldehyde groups formed on the polysaccharide matrix during the periodate oxidation reaction can be used to covalently bond amine containing biologics and therapeutic agents.
• the combination of such biologics, drugs and agents with wound dressings of the present invention using the aldehyde-modified regenerated cellulose substrates can provide improved hemostatic wound dressings, wound healing dressings, drug delivery devices, and tissue engineering matrices.
• a 15.75 g piece of Nu-Knit® rayon fabric was cut in the form of a strip 1.5 inches wide.
• the strip was wound on a mandrel and suspended in 600 ml of aqueous isopropyl alcohol (IPA) (200 ml IPA/400 ml de-ionized (DI) water).
• IPA aqueous isopropyl alcohol
• DI de-ionized water
• the mandrel with the oxidized fabric was washed for 30 minutes in 1 liter of cold DI water containing 50 ml of ethylene glycol. It was then washed with aqueous IPA (50/50) for 15 minutes, followed by a pure IPA wash for 15 minutes.
• a 10 g piece of cellulose rayon non-woven fabric was cut in the form of a rectangle and placed in an aqueous solution of sodium periodate (Aldrich, Milwaukee, 53201) (1:0.7 molar ratio).
• the fabric was placed in a container modified to exclude light and soaked in the dark for 24 hours at 37° C. The solution was discarded after the reaction.
• the fabric was repeatedly washed with DI water until the pH was 6-7. It was then washed with aqueous IPA (50/50) for 15 minutes. The fabric then was washed in pure IPA for 15 minutes.
• the fabric was dried in ambient air for several hours. [aldehyde content: 51.04%]
• a porcine spleen incision model was used for hemostasis evaluation.
• the materials were cut into 2.5 cm ⁇ 2.0 cm rectangles.
• a linear incision of 1.5 cm with a depth of 1.0 cm was made with a surgical blade on a porcine spleen.
• digital tamponade was applied to the incision for 2 minutes.
• the hemostasis was then evaluated. Additional applications of digital tamponade for 30 seconds each were used until complete hemostasis was achieved.
• the fabrics providing hemostasis within 15 minutes, preferably within 12 minutes, were considered to be effective hemostats.
• Wound dressings comprising aldehyde-modified regenerated cellulose achieved rapid hemostasis compared to the negative control of surgical gauze.
• B is the burette reading (in ml) from a blank titration
• S is the burette reading (in ml) from a sample
• W is the sample weight.
• Aldehyde content is the number of glucose rings (by mole) containing the dialdehyde functionality.
• Aldehyde content of aldehyde modified regenerated cellulose in the present invention, processed in various physical forms, is substantially consistent in the range of 20-50%.
• MRSA Methicillin-resistant Staphylococcus aureus organisms were grown in Trypticase Soy Broth (TSB) for 24 hours at 30-35° C. Trypticase Soy Agar (TSA) and TSB were the media used in this study. The dilutions used 0.85% saline. All media and solutions were sterile.

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• 2002
  • 2002-11-26 US US10/305,040 patent/US20040101548A1/en not_active Abandoned
• 2003
  • 2003-06-27 BR BR0304601A patent/BR0304601A/pt not_active Application Discontinuation
  • 2003-06-27 CA CA 2433994 patent/CA2433994A1/en not_active Abandoned
  • 2003-06-27 TW TW92117744A patent/TW200408416A/zh unknown
  • 2003-06-27 EP EP20030254080 patent/EP1424085A1/en not_active Withdrawn
  • 2003-06-27 JP JP2003185594A patent/JP2004174222A/ja active Pending
  • 2003-06-27 AU AU2003205016A patent/AU2003205016A1/en not_active Abandoned
  • 2003-06-27 CN CNA03152687XA patent/CN1502374A/zh active Pending
  • 2003-06-27 AR ARP030102344 patent/AR040304A1/es unknown
  • 2003-06-28 KR KR1020030042973A patent/KR20040047537A/ko not_active Application Discontinuation
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